Canonical Allele Identifier: CA6927656
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs778901831
ExAC: 13:28498374 C / G
gnomAD v2: 13-28498374-C-G
gnomAD v4: 13-27924237-C-G
MyVariant Identifiers: chr13:g.28498374C>G (hg19) chr13:g.27924237C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924237C>G , CM000675.2:g.27924237C>G GRCh38
NC_000013.10:g.28498374C>G , CM000675.1:g.28498374C>G GRCh37
NC_000013.9:g.27396374C>G NCBI36
NG_008183.1:g.9207C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-19C>G MANE Select ENSP00000370421.4:n.407-19C>G
ENST00000381033.4:c.407-19C>G ENSP00000370421.4:n.407-19C>G
NM_000209.3:c.407-19C>G NP_000200.1:n.407-19C>G
XR_941578.1:n.3534-19C>G
XR_941579.1:n.2133-19C>G
XR_941580.1:n.1049-19C>G
XR_941578.2:n.3546-19C>G
XR_941580.2:n.1061-19C>G
NM_000209.4:c.407-19C>G MANE Select NP_000200.1:n.407-19C>G
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